低滴度烟碱乙酰胆碱受体神经节抗体患者的死后研究:对临床神经系统疾病的意义

D. Younger
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引用次数: 1

摘要

小纤维多神经病变是一种公认的由躯体感觉传入和自主传出神经纤维减轻的综合征,它们分别介导皮肤的疼痛、冷热温度传入和自主传出功能。神经乙酰胆碱受体神经节抗体血清滴度低和自主神经衰竭的患者,在自身免疫性痴呆、脑病和前列腺癌的背景下,出现症状性小纤维多神经病变。在常规电诊断和自主神经实验室检查以及小腿和大腿的表皮神经纤维分析中检测到大纤维和小纤维多神经病和自主神经异常。静脉注射免疫球蛋白治疗后一年的临床改善先于临床神经认知功能下降和死亡。死后检查显示阿尔茨海默病的典型特征,周围神经系统有神经性神经病理改变,存活的自主神经节与突触后神经元nachr的通道病变机制一致。
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A Postmortem Study of a Patient with Low Titer Nicotinic Acetylcholine Receptor Ganglionic Antibody: Implications for Clinical Neurologic Disease
Small fiber polyneuropathy is a well-recognized syndrome mitigated by somatic sensory afferent and autonomic efferent nerve fibers that respectively mediate pain, heat and cold temperature afferent and autonomic efferent function in the skin. A patient with low serum titers of neuronal acetylcholine receptor ganglionic antibodies and autonomic failure had symptomatic small fiber polyneuropathy late in life in the setting of autoimmune dementia and encephalopathy and prostate cancer. Large and small fiber polyneuropathy and dysautonomia were detected in routine electrodiagnostic and autonomic laboratory studies, and epidermal nerve fiber analysis of the calf and thigh. Clinical improvement for one year concomitant with intravenous immune globulin therapy preceded a clinical decline in neurocognitive function and death. Postmortem examination showed typical features of Alzheimer disease with neuropathic neuropathological changes in the peripheral nervous system, and viable autonomic ganglia consistent with a channelopathy mechanism involving postsynaptic neuronal nAChRs.
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